QRD Template
The EU's standard template for how a medicine's product information has to be laid out.
The QRD Template (Quality Review of Documents template) is the standard format the European Medicines Agency requires for a medicine's product information: the Summary of Product Characteristics, the labeling, and the PIL. It fixes the section order, the headings, and in places the required wording, across every centrally authorized product in the EU, so a PIL for one medicine reads in a structure a pharmacist or patient anywhere in the EU would recognize from another.
It's worth knowing specifically because it has no direct equivalent in the US. The FDA's PI follows its own required structure under the Physician Labeling Rule, but that's a different format built for a different audience (clinicians, not patients) under a different regulator. A company running labeling or promotional content across both markets can't reuse one region's template for the other. The QRD template only governs the EU side.